Anticarcinogenic effects of diet-related apoptosis in the colorectal mucosa

被引:73
作者
Johnson, IT [1 ]
机构
[1] Inst Food Res, Norwich NR4 7UA, Norfolk, England
关键词
gastrointestinal tract; cancer; apoptosis; diet; PUFA; phytochemicals;
D O I
10.1016/S0278-6915(02)00051-0
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The crypt is the fundamental unit of epithelial proliferation in the intestinal mucosa. The progeny of the pluripotent stem cells located near the base of the crypt migrate towards the crypt orifice, divide once or twice more, and then undergo differentiation, senescence and exfoliation. Programmed cell death (apoptosis) also occurs deep in the proliferative zone. Various lines of evidence suggest that apoptosis provides a protective mechanism against neoplasia by removing genetically damaged stem cells from the epithelium before they can undergo clonal expansion. Several different classes of food constituents, including certain polyunsaturated fatty acids, the short-chain fatty acid butyrate, and some phytochemicals including flavonoids and glucosinolates breakdown products, can modulate both cellular proliferation and programmed death. Each of these food components has also been shown to suppress the emergence of aberrant crypt foci in animal models of carcinogenesis. Further mechanistic and clinical studies are required to establish whether such dietary effects can be exploited to achieve preventive or therapeutic effects in humans. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1171 / 1178
页数:8
相关论文
共 70 条
[1]   Apoptosis [J].
Afford, S ;
Randhawa, S .
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 2000, 53 (02) :55-63
[2]  
AUGERON C, 1984, CANCER RES, V44, P3961
[3]   Apoptosis cascade proteins are regulated in vivo by high intracolonic butyrate concentration: Correlation with colon cancer inhibition [J].
Avivi-Green, C ;
Polak-Charcon, S ;
Madar, Z ;
Schwartz, B .
ONCOLOGY RESEARCH, 2000, 12 (02) :83-95
[4]   Stem cells: the intestinal stem cell as a paradigm [J].
Bach, SP ;
Renehan, AG ;
Potten, CS .
CARCINOGENESIS, 2000, 21 (03) :469-476
[5]  
BARNARD JA, 1993, CELL GROWTH DIFFER, V4, P495
[6]   CELL-DEATH IN HEALTH AND DISEASE - THE BIOLOGY AND REGULATION OF APOPTOSIS [J].
BELLAMY, COC ;
MALCOMSON, RDG ;
HARRISON, DJ ;
WYLLIE, AH .
SEMINARS IN CANCER BIOLOGY, 1995, 6 (01) :3-16
[7]   Slow-release pellets of sodium butyrate do not modify azoxymethane (AOM)-induced intestinal carcinogenesis in F344 rats [J].
Caderni, G ;
Luceri, C ;
De Filippo, C ;
Salvadori, M ;
Giannini, A ;
Tessitore, L ;
Dolara, P .
CARCINOGENESIS, 2001, 22 (03) :525-527
[8]   Signalling apoptosis: a radical approach [J].
Carmody, RJ ;
Cotter, TG .
REDOX REPORT, 2001, 6 (02) :77-90
[9]   Involvement of p21Waf1/Cip1 and its cleavage by DEVD-caspase during apoptosis of colorectal cancer cells induced by butyrate [J].
Chai, F ;
Evdokiou, A ;
Young, GP ;
Zalewski, PD .
CARCINOGENESIS, 2000, 21 (01) :7-14
[10]   Mechanisms underlying nonsteroidal antiinflammatory drug-mediated apoptosis [J].
Chan, TA ;
Morin, PJ ;
Vogelstein, B ;
Kinzler, KW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (02) :681-686